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WormBase Tree Display for Variation: WBVar00100993

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Name Class

WBVar00100993NamePublic_nameWBVar00100993
Other_namepas5852
cewivar00109402
F40F12.5a.1:c.747+53A>G
HGVSgCHROMOSOME_III:g.9909035T>C
Sequence_detailsSMapS_parentSequenceF40F12
Flanking_sequencestttcattattcgagcaagagactccaattttttttcgattttcaaaaaaattcgtttttttttttaattaaagccggaaaattgactttgtcagagcggaatttacagaggcctagcaaaaaatgtgactcgtgggccattaattcctatcccattatattattttcaagaaacttataagttagtcatgccatcggaatttcaatcagtcacgtgtgacagtctaattctgaatacaaggagacgcccatttctcgtctgcgtctctttattttgaattcgttgttttatttttcttttttttggttaaaaactagattcctttgagaaacatataatttcaaatacttaccacttccacagaaacagaatcgccaattttcagattcagaatgaaattgaaccattcgaaattttgataaacttctattcgtttctctacactgacagccagaagatgtctgaaaagggaaaaaattttatttataaagataataaatatacattgcttgatcttggtttattctcattacatcggatctggtaatcattgcacaaatcagaggagtgcagtcgagttcctgaaatttaaaaaaattg
Mapping_targetF40F12
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (57)
PersonWBPerson6900
AnalysisWGS_Pasadena_Quinlan
Million_mutation_project_reanalysis
WGS_Andersen
HistoryAcquires_mergeWBVar01447742
StatusLive
AffectsGeneWBGene00009594
TranscriptF40F12.5a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF40F12.5a.1:c.747+53A>G
Intron_number7/18
MethodWGS_Pasadena_Quinlan